Background
Bisphenol-A (BPA) is a widespread
pollutant whose effects on pregnant women are poorly understood. Therefore, we investigated the effects of BPA on basal and bacteria-stimulated production of proinflammatory
cytokines [
interleukin (IL)-1β,
tumor necrosis factor-α (TNF-α) and IL-6], anti-inflammatory mediators [
soluble glycoprotein 130 (sgp) 130,
heme oxidase-1 (HO-1) and IL-10] and
biomarkers for neurodevelopment [
brain-derived neurotrophic factor (
BDNF)], and oxidative stress [8-
isoprostane (8-IsoP)] by the placenta. Methods Placental explant cultures were treated with BPA (0-10,000 nM) in the presence or absence of 107 colony-forming unit (CFU)/mL heat-killed Escherichia coli for 24 h.
Biomarker concentrations in
conditioned medium were quantified by the
enzyme-linked
immunosorbent assay (ELISA). Results Under basal conditions, IL-1β and
IL-6 production was enhanced by BPA in a dose-dependent manner.
Sgp130, a soluble receptor that reduces
IL-6 bioactivity, was suppressed by BPA at 1000-10,000 nM. BPA also enhanced
BDNF production at 1000 and 10,000 nM, and 8-IsoP expression
at 10 and 100 nM. For bacteria-treated cultures, BPA increased
IL-6 production at 100 nM and reduced
sgp130 at 1000 nM but had no effect on IL-1β, TNF-α,
BDNF, HO-1, 8-IsoP or
IL-10 production. Conclusion BPA may increase placental
inflammation by promoting IL-1β and
IL-6 but inhibiting
sgp130. It may also disrupt oxidative balance and neurodevelopment by increasing 8-IsoP and
BDNF production.